JP2007216657A - Moisture-permeable waterproof fabric and its manufacturing method - Google Patents

Moisture-permeable waterproof fabric and its manufacturing method Download PDF

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JP2007216657A
JP2007216657A JP2006043217A JP2006043217A JP2007216657A JP 2007216657 A JP2007216657 A JP 2007216657A JP 2006043217 A JP2006043217 A JP 2006043217A JP 2006043217 A JP2006043217 A JP 2006043217A JP 2007216657 A JP2007216657 A JP 2007216657A
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moisture
permeable waterproof
waterproof fabric
calcium carbonate
urethane resin
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JP4731351B2 (en
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Yutaka Hayashi
豊 林
Yasunao Shimano
泰尚 嶋野
Hiroki Osugi
裕樹 大杉
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Komatsu Seiren Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a moisture-permeable waterproof fabric which is inexpensive and can be easily manufactured, while having an excellent moisture-permeable waterproof property. <P>SOLUTION: The moisture-permeable waterproof fabric comprises a urethane resin coated film containing a finely porous film formed on at least one surface of a fiber fabric wherein the finely porous film contains calcium carbonate particles. The content of the calcium carbonate particles contained based on 100 pts.mass of the urethane resin forming the finely porous film is 10 to 100 pts.mass by a mass ratio. The average particle diameter of the calcium carbonate is 0.05 to 5 μm. <P>COPYRIGHT: (C)2007,JPO&INPIT

Description

本発明は、透湿性防水布帛およびその製造方法に関するものである。 The present invention relates to a moisture-permeable waterproof fabric and a method for producing the same.

合羽やスキ−ウエア−、ウインドブレ−カ−をはじめ、テント、靴材など湿気を通過させるが、雨などの水の進入を防止する素材として透湿性防水布帛は様々なものに使用されている。
このような透湿性防水布帛として、例えば、繊維布帛の片面に、ポリウレタン重合体の樹脂溶液をコ−テイングし、湿式凝固して得られた微多孔質膜を有するコ−テイング加工布(特許文献1)や繊維布帛の片面にウレタン樹脂の無孔質膜を貼り合せて得られた透湿性防水布帛(特許文献2)が知られている。
Moisture such as knitted feathers, ski wear, windbreakers, tents, and shoe materials are allowed to pass through, but moisture-permeable waterproof fabrics are used for various materials as materials that prevent the entry of water such as rain. .
As such a moisture-permeable waterproof fabric, for example, a coated fabric having a microporous film obtained by coating a polyurethane polymer resin solution on one side of a fiber fabric and wet coagulating (Patent Document) 1) and a moisture-permeable waterproof fabric (Patent Document 2) obtained by bonding a non-porous film of urethane resin to one side of a fiber fabric is known.

特に、湿式凝固して得えられた微多孔質膜は、無孔質膜を貼り合わせたものに比べ、一般に、JIS L1099塩化カルシウム法(A−1法)にて測定した透湿度は優れたものが得られやすいが、防水性や酢酸カリウム法(JIS L1099B−1法)による透湿度がやや低く、より高い透湿性や防水性が望まれている。 In particular, the microporous membrane obtained by wet coagulation is generally superior in moisture permeability measured by the JIS L1099 calcium chloride method (A-1 method) as compared with a nonporous membrane laminated. Although it is easy to obtain, water resistance and water permeability by the potassium acetate method (JIS L1099B-1 method) are slightly low, and higher moisture permeability and water resistance are desired.

そのため、樹脂層中にN,N−ジメチルホルムアミドの吸油量が350ミリリットル/100g以上の平均粒子径が0.016μmの疎水性二酸化ケイ素を含有させることにより、塩化カルシウム法による透湿度9820g/m/24h、耐水圧1.12kgf/cm(112kPa)の透湿性防水布帛が知られている。(特許文献3)。
特開昭55−80583 特開平7−9631 特開平6−272168
Therefore, by incorporating hydrophobic silicon dioxide having an average particle size of 0.016 μm and an oil absorption of N, N-dimethylformamide of 350 ml / 100 g or more into the resin layer, the moisture permeability by the calcium chloride method is 9820 g / m 2. A moisture-permeable waterproof fabric having a water pressure resistance of 1.12 kgf / cm 2 (112 kPa) is known. (Patent Document 3).
JP-A-55-80583 JP-A-7-9631 JP-A-6-272168

しかしながら、N,N−ジメチルホルムアミドの吸油量が350ミリリットル/100g以上であり平均粒子径が0.016μmの疎水性二酸化ケイ素は、特殊な粒子であるため価格が高く、得られる透湿性防水布帛が非常に高価になってしまうとの問題があった。また、平均粒子径が1μm以上の粒子を用いると効果が得られない(引用文献3 比較例1)との記載もみられ、粒子径の管理が厳しく、このような小さな微粒子を樹脂膜中に維持することは、粒子の凝集などの対策も含め、生産上、手間がかかる上に、透湿性や防水性などの性能の安定化も非常に困難であった。
したがって、本発明では、優れた透湿性、防水性を有していながら、安価で、生産が容易である透湿性防水布帛を提供することを目的としている。
However, hydrophobic silicon dioxide having an oil absorption amount of N, N-dimethylformamide of 350 ml / 100 g or more and an average particle size of 0.016 μm is a special particle and is expensive, and the resulting moisture-permeable waterproof fabric is obtained. There was a problem that it would be very expensive. In addition, the use of particles having an average particle diameter of 1 μm or more is not effective (Cited Document 3 Comparative Example 1), the particle diameter is strictly controlled, and such small particles are maintained in the resin film. In addition to taking measures such as agglomeration of particles, it takes time and effort in production, and it is very difficult to stabilize performance such as moisture permeability and waterproofness.
Accordingly, an object of the present invention is to provide a moisture-permeable waterproof fabric that is inexpensive and easy to produce while having excellent moisture permeability and waterproofness.

本発明者らは、上記課題を解決するために鋭意検討の結果、本発明をするに至った。
すなわち、本発明は、以下の構成(1)〜(7)からなる。
As a result of intensive studies in order to solve the above problems, the present inventors have come up with the present invention.
That is, this invention consists of the following structures (1)-(7).

(1)繊維布帛の少なくとも片面に微多孔質膜を含むウレタン樹脂被膜が形成された透湿性防水布帛であって、前記微多孔質膜中に炭酸カルシウム粒子を含むことを特徴とする透湿性防水布帛。
(2)前記微多孔質膜を形成するウレタン樹脂100質量に対し、前記炭酸カルシウム粒子が質量比で10質量部〜100質量部含むことを特徴とする上記(1)に記載の透湿性防水布帛。
(3)前記炭酸カルシウム粒子の平均粒子径が0.05μm〜5μmであることを特徴とする上記(1)または(2)に記載の透湿性防水布帛。
(4)前記微多孔質膜中に、酸化アルミニウム微粒子もしくは酸化ケイ素微粒子をも含むことを特徴とする上記(1)〜(3)のいずれかに記載の透湿性防水布帛。
(1) A moisture-permeable waterproof fabric in which a urethane resin coating including a microporous membrane is formed on at least one surface of a fiber fabric, wherein the microporous membrane includes calcium carbonate particles. Fabric.
(2) The moisture-permeable waterproof fabric according to (1), wherein the calcium carbonate particles are included in a mass ratio of 10 to 100 parts by mass with respect to 100 parts by mass of the urethane resin forming the microporous membrane. .
(3) The moisture-permeable waterproof fabric according to (1) or (2) above, wherein the calcium carbonate particles have an average particle diameter of 0.05 μm to 5 μm.
(4) The moisture-permeable waterproof fabric according to any one of (1) to (3) above, wherein the microporous membrane also contains aluminum oxide fine particles or silicon oxide fine particles.

(5)前記炭酸カルシウム100質量部に対し、前記アルミニウム微粒子もしくは前記二酸化ケイ素微粒子が質量比で0.1〜30質量部含むことを特徴とする上記(4)に記載の透湿性防水布帛。
(6)耐水圧が100kPa以上200kPa以下であり、塩化カルシウム法による透湿度が8000g/m・24hrs以上15000g/m・24hrs以下であり、酢酸カリウム法による透湿度が10000g/m・24hrs以上30000g/m・24hrs以下であることを特徴とする上記(1)〜(5)のいずれかに記載の透湿性防水布帛。
(7)繊維布帛に、炭酸カルシウム粒子を含むウレタン樹脂溶液を塗布した後、水中に浸漬し、ウレタン樹脂を凝固させることを特徴とする透湿性防水布帛の製造方法。
(5) The moisture-permeable waterproof fabric according to (4) above, wherein the aluminum fine particles or the silicon dioxide fine particles contain 0.1 to 30 parts by mass with respect to 100 parts by mass of the calcium carbonate.
(6) Water pressure is below 200kPa than 100 kPa, the moisture permeability by the calcium chloride method is not more than 8000g / m 2 · 24hrs or more 15000g / m 2 · 24hrs, water vapor permeability with potassium acetate method is 10000g / m 2 · 24hrs The moisture-permeable waterproof fabric according to any one of (1) to (5) above, which is 30000 g / m 2 · 24 hrs or less.
(7) A method for producing a moisture-permeable waterproof fabric, characterized in that a urethane resin solution containing calcium carbonate particles is applied to a fiber fabric and then immersed in water to solidify the urethane resin.

本発明の透湿性防水布帛は、優れた透湿性と防水防水性を有していながら、製造が容易である。したがって、安価に、優れた透湿性と防水性を有する透湿性防水布帛を提供することができ、本発明の透湿性防水布帛をウインドブレ−カ−、コ−ト、ジャケット、スキ−ウエア−、スノ−ボ−ドウエア−、テントなどに用いれば、使用者に安価で快適な環境を提供することができる。   The moisture-permeable waterproof fabric of the present invention is easy to manufacture while having excellent moisture permeability and waterproof property. Therefore, a moisture-permeable waterproof fabric having excellent moisture permeability and waterproofness can be provided at low cost, and the moisture-permeable waterproof fabric of the present invention can be used as a windbreaker, coat, jacket, skiwear, If used for snowboard wear, tents, etc., it is possible to provide a user with an inexpensive and comfortable environment.

本発明の透湿性防水布帛は、繊維布帛の少なくとも片面に微多孔質膜を含むウレタン樹脂被膜が形成された透湿性防水布帛であって、前記微多孔質膜中に炭酸カルシウム粒子を含むものであるが、本発明に有用な繊維布帛の素材は、ポリエステル、ナイロン、アクリル、ポリウレタン、アセテ−ト、レ−ヨン、ポリ乳酸などの化学繊維、綿、麻、絹、羊毛等の天然繊維やこれらの混繊、混紡、交織品であってもよく、特に限定されるものではない。また、それらは織物、編物、不織布等いかなる形態であってもよい。
また、繊維布帛は、染色、捺染をはじめ、制電加工、撥水加工、抗菌防臭加工、制菌加工、紫外線遮蔽加工などを施してあってもよい。
The moisture-permeable waterproof fabric of the present invention is a moisture-permeable waterproof fabric in which a urethane resin coating including a microporous membrane is formed on at least one surface of a fiber fabric, and the calcium porous particles are included in the microporous membrane. The fiber fabric material useful in the present invention includes polyester, nylon, acrylic, polyurethane, acetate, rayon, polylactic acid and other chemical fibers, cotton, hemp, silk, wool and other natural fibers, and mixtures thereof. It may be a textile, a blend, or a woven product, and is not particularly limited. Further, they may be in any form such as woven fabric, knitted fabric, non-woven fabric.
The fiber fabric may be subjected to dyeing and printing, antistatic processing, water repellent processing, antibacterial and deodorizing processing, antibacterial processing, ultraviolet shielding processing, and the like.

本発明の微多孔質膜とは、表面に約1μm以下の微細孔を有し、内部には10〜50μm程度の空孔を有し、その壁面にはさらに孔が形成され、互いに連通した構造を有している。
また、微多孔質膜の厚みは、10〜100μm程度であるものがよく、10μm未満では耐水圧が低く、また、100μmを超えると得られる透湿性防水布帛の風合が硬くなる。
また、ウレタン樹脂とは、微多孔質膜を形成されるウレタン樹脂であればエ−テル系、エステル系、エ−テル・エステル系、ポリカ−ボネ−ト系等特に限定されるものではなく任意選択すれば良いが、湿式法にて製造した際に、微多孔質膜を形成するものが好ましく用いられ、特にエステル系ポリウレタン樹脂が用いられる。
The microporous membrane of the present invention has a structure having fine pores of about 1 μm or less on the surface, pores of about 10 to 50 μm inside, further pores formed on the wall surface, and communication with each other have.
The thickness of the microporous membrane is preferably about 10 to 100 μm, and if it is less than 10 μm, the water pressure resistance is low, and if it exceeds 100 μm, the moisture-permeable waterproof fabric obtained becomes hard.
The urethane resin is not particularly limited as long as it is a urethane resin for forming a microporous film, and is not limited to ether, ester, ether-ester, polycarbonate, etc. What is necessary is just to select, but when manufacturing by a wet method, what forms a microporous film | membrane is used preferably, and ester-type polyurethane resin is used especially.

本発明の微多孔質膜は、微多孔質膜中に炭酸カルシウム粒子を含むものである。
このとき用いられる炭酸カルシウム粒子は、石灰岩を粉砕して得られる重質炭酸カルシウム、化学的に製造される沈降炭酸カルシウムが挙げられる。また、その粒子径も平均粒子径で0.01μm〜50μm程度のものが使用でき、一次粒子の状態のものやこれらの2次の凝集物などであってもよい。また、形状も、針状、柱状、防錘状、立方状、球状、板状、曲玉上、連鎖状やこれらの凝集物や不定形であってもよく特に限定されない。
また、これらの表面は、脂肪酸、樹脂等で表面処理が施されていてもよい。
さらに、炭酸カルシウム粒子は、上記の凝集したものを、ジメチルホルムアミド溶剤やビヒクルとしてウレタン樹脂、また、分散剤などを加えて、ディパ−サ−などでプレミックスし、サンドミル、三本ロ−ルミル、ビ−ズミルなどで平均粒子径0.05〜5μmに粉砕したものを使用するのがより好ましい。
The microporous membrane of the present invention includes calcium carbonate particles in the microporous membrane.
Examples of the calcium carbonate particles used at this time include heavy calcium carbonate obtained by pulverizing limestone and chemically produced precipitated calcium carbonate. Further, the average particle diameter of about 0.01 μm to 50 μm can be used, and the particles may be in the form of primary particles or secondary aggregates thereof. Also, the shape may be a needle shape, a column shape, a weight-proof shape, a cubic shape, a spherical shape, a plate shape, a curved ball shape, a chain shape, an aggregate or an indeterminate shape thereof, and is not particularly limited.
Further, these surfaces may be subjected to a surface treatment with a fatty acid, a resin or the like.
Further, the calcium carbonate particles are obtained by premixing the agglomerated particles with a urethane resin as a dimethylformamide solvent or a vehicle, a dispersant, and the like with a dither, etc., a sand mill, a three-roll mill, It is more preferable to use a powder that has been pulverized to a mean particle size of 0.05 to 5 μm with a bead mill.

また、炭酸カルシウム粒子の含有量は、微多孔質膜を形成するウレタン樹脂100質量部に対し、炭酸カルシウム粒子が質量比で10質量部〜100質量部含むとよい。より好ましくは、40質量部〜70質量部が好ましい。一般的には樹脂中に多量の無機粒子を添加すると、得られる膜が脆くなり、耐水圧の低下や風合が硬化すると考えられていたが、本発明の炭酸カルシウムでは、他の無機化合物に比べ、膜に膨らみ感が増すとともに耐水圧を低下させずに、塩化カルシウム法、酢酸カルシウム法による透湿度も優れたものをえることができる。   Further, the content of the calcium carbonate particles is preferably 10 to 100 parts by mass of the calcium carbonate particles by mass ratio with respect to 100 parts by mass of the urethane resin forming the microporous membrane. More preferably, 40 mass parts-70 mass parts are preferable. In general, it was thought that when a large amount of inorganic particles was added to the resin, the resulting film became brittle and the water pressure resistance decreased and the texture was cured. However, in the calcium carbonate of the present invention, other inorganic compounds are used. In comparison, it is possible to obtain a film having a feeling of swelling and an excellent moisture permeability by the calcium chloride method and the calcium acetate method without decreasing the water pressure resistance.

本発明では、さらに微多孔質膜中に、酸化アルミニウム、二酸化ケイ素などの微粒子の少なくとも一つを含むとよい。特に、酸化アルミニウムもしくは二酸化ケイ素が好ましい。
酸化アルミニウムとしては、乾式法の燃焼法もしくはア−ク法で製造された平均一次粒子径が0.05μm以下のものが凝集し、0.1〜50μm程度の大きさとなったものが好ましい。
また、二酸化ケイ素としては、乾式の燃焼法やア−ク法で製造された平均一次粒子径が0.05μm以下であり、これらのものが0.1〜50μm程度の大きさに凝集したもの、また、湿式法の沈降法やゲル法で製造されたもので、一次粒子径が、0.05μm以下であり、これらのものが0.1〜50μm程度の大きさに凝集したものが使用できる。
また、これらの表面が、メチル基、トリメチルシリル基、ジメチルシリコ−ン基などで疎水性処理されたものであってもよい。
さらに、酸化アルミニウム微粒子や二酸化ケイ素微粒子は、上記の凝集したものを、ジメチルホルムアミド溶剤やビヒクルとしてウレタン樹脂、また、分散剤などを加えて、ディパ−サ−などでプレミックスし、サンドミル、三本ロ−ルミル、ビ−ズミルなどで平均粒子径0.05〜5μmに粉砕したものを使用するのが好ましい。
In the present invention, the microporous film may further include at least one of fine particles such as aluminum oxide and silicon dioxide. In particular, aluminum oxide or silicon dioxide is preferable.
As the aluminum oxide, those having an average primary particle size of 0.05 μm or less produced by a dry combustion method or an arc method are preferably aggregated to a size of about 0.1 to 50 μm.
Moreover, as silicon dioxide, the average primary particle diameter produced by a dry combustion method or an arc method is 0.05 μm or less, and these are aggregated to a size of about 0.1 to 50 μm, Moreover, what was manufactured by the precipitation method of the wet method and the gel method, and a primary particle diameter is 0.05 micrometer or less, and these things aggregated to the magnitude | size of about 0.1-50 micrometers can be used.
These surfaces may be subjected to a hydrophobic treatment with a methyl group, a trimethylsilyl group, a dimethylsilicone group or the like.
Further, the aluminum oxide fine particles and silicon dioxide fine particles are pre-mixed with a urethane resin or a dispersant as a dimethylformamide solvent or vehicle and premixed with a disperser etc. It is preferable to use a product pulverized to an average particle size of 0.05 to 5 μm by a roll mill, a bead mill or the like.

これらの微粒子の添加量は、前記炭酸カルシウム100質量部に対し、微粒子が質量比で0.1〜30質量部含むとよい。
前記炭酸カルシウム粒子にこれらの粒子を添加することにより、耐水圧や塩化カルシウム法による透湿性を実質低下させずに、酢酸カルシウム法による透湿性を向上させることができる。
The addition amount of these fine particles is preferably 0.1 to 30 parts by mass with respect to 100 parts by mass of the calcium carbonate.
By adding these particles to the calcium carbonate particles, the moisture permeability by the calcium acetate method can be improved without substantially reducing the water pressure resistance or moisture permeability by the calcium chloride method.

本発明の微多孔質膜を含むポリウレタン樹脂被膜とは、前記微多孔質膜のみからなるものであってもよく、また、微多孔質膜の片面に耐水圧向上の目的や柄の付与、すべり性の向上を目的にて他のウレタン樹脂膜を全面または点状や線状など部分的に有していてもよい。
また、微多孔質膜を含むポリウレタン樹脂被膜の厚みは、10〜100μmであるとよく、10μm未満では耐水圧が低く、また、100μmを超えると得られる透湿性防水布帛の風合が硬くなる。
本発明の透湿性防水布帛は、前記微多孔質膜を含むポリウレタン樹脂被膜が繊維布帛の片面または両面に形成されている。
The polyurethane resin coating containing the microporous membrane of the present invention may be composed only of the microporous membrane. Also, the purpose of improving the water pressure resistance, imparting a pattern, or slipping on one side of the microporous membrane. Other urethane resin films may be provided on the entire surface or partially in the form of dots or lines for the purpose of improving the properties.
Further, the thickness of the polyurethane resin film including the microporous film is preferably 10 to 100 μm, and if it is less than 10 μm, the water pressure resistance is low, and if it exceeds 100 μm, the moisture-permeable waterproof fabric obtained becomes hard.
In the moisture-permeable waterproof fabric of the present invention, the polyurethane resin coating containing the microporous membrane is formed on one side or both sides of the fiber fabric.

本発明における透湿性防水布帛では、用途に応じ求められる透湿性や耐水圧を有するものを得れば良いが、ウレタン樹脂被膜として、微多孔質膜のみからなるもの、または、微多孔質膜上に部分的他のウレタン樹脂膜を付与したもので、耐水圧が100kPa以上200kPa以下であり、塩化カルシウム法による透湿度が8000g/m・24hrs以上15000g/m・24hrs以下であり、酢酸カリウム法による透湿度が10000g/m・24hrs以上30000g/m・24hrs以下のものをえることができる。 In the moisture-permeable waterproof fabric in the present invention, it is only necessary to obtain one having moisture permeability and water pressure required depending on the application. However, as the urethane resin film, the urethane resin film consists only of a microporous film, or on a microporous film. In addition, the water pressure is 100 kPa or more and 200 kPa or less, the moisture permeability by the calcium chloride method is 8000 g / m 2 · 24 hrs or more and 15000 g / m 2 · 24 hrs or less, potassium acetate moisture permeability can be obtained as 10000g / m 2 · 24hrs or more 30 000 g / m of 2 · 24hrs or less by law.

耐水圧が200kPaを超えると透湿性が低下する可能性があり、また、塩化カルシウム法での透湿度が15000g/m・24hrs、酢酸カリウム法での透湿度が30000g/m・24hrsを超えると耐水圧が低下する恐れがある。
ただし、特に、耐水圧が、200kPa以上が要求される分野では、微多孔質膜の全面にポリウレタン樹脂からなる無孔質膜を付与するとよい。
ここでいう塩化カルシウム法による透湿度とは、JIS L1099−1993B−1法にて測定した値をいう。また、塩化カルシウム法とは、JIS L1099−1993A−1法にて測定した値をいう。なお、塩化カルシウム法、酢酸カルシウム法ともに、24時間当りの透湿量に換算したものをいう。
If the water pressure resistance exceeds 200 kPa, the moisture permeability may decrease, the moisture permeability in the calcium chloride method may exceed 15000 g / m 2 · 24 hrs, and the moisture permeability in the potassium acetate method may exceed 30000 g / m 2 · 24 hrs. There is a risk that the water pressure will decrease.
However, in particular, in a field where the water pressure resistance is required to be 200 kPa or more, a nonporous film made of a polyurethane resin may be provided on the entire surface of the microporous film.
The moisture permeability by the calcium chloride method here refers to a value measured by the JIS L1099-1993B-1 method. The calcium chloride method refers to a value measured by the JIS L1099-1993A-1 method. The calcium chloride method and the calcium acetate method are both converted to moisture permeation per 24 hours.

また、耐水圧は、JIS L1092−1998耐水度試験(静水圧法)B法(高水圧法)に準じた方法で測定した値をいう。なお、水圧をかけることにより試験片が伸びる場合には、試験片の上にナイロンタフタ(2.54cm当りの縦糸と横糸の密度の合計が210本程度のもの)を重ねて、試験機に取り付けて測定をおこなった。   The water pressure resistance is a value measured by a method according to JIS L1092-1998 water resistance test (hydrostatic pressure method) B method (high water pressure method). When the test piece is stretched by applying water pressure, a nylon taffeta (with a total of about 210 warps and wefts per 2.54 cm) is stacked on the test piece and attached to the testing machine. And measured.

次に本発明の好ましい一製造方法に従いさらに詳細に本発明を説明する。
本発明の透湿性防水布帛の好ましい製造方法は、繊維布帛に、炭酸カルシウム粒子を含むウレタン樹脂溶液を塗布した後、水中に浸漬し、ウレタン樹脂を凝固させるとよい。
繊維布帛は、精練、染色、捺染をはじめ、制電加工、撥水加工、抗菌防臭加工、制菌加工、紫外線遮蔽加工、カレンダ−加工などを必要に応じ施してあってもよい。
Next, the present invention will be described in more detail according to one preferred production method of the present invention.
The preferable manufacturing method of the moisture-permeable waterproof fabric of this invention is good to apply | coat the urethane resin solution containing a calcium carbonate particle to a fiber fabric, and to immerse in water and to solidify a urethane resin.
The fiber fabric may be subjected to scouring, dyeing, printing, antistatic processing, water repellent processing, antibacterial deodorization processing, antibacterial processing, ultraviolet shielding processing, calendar processing, and the like as necessary.

繊維布帛に塗布する炭酸カルシウム粒子を含むウレタン樹脂溶液とは、前記のウレタン樹脂と炭酸カルシウム粒子を含み、溶媒として、ジメチルホルムアミド(以下、DMF)、ジメチルアセトアミド、N−メチルピロリドンなどの水溶性の極性有機溶媒を主体とするものが好ましく選択される。
前記炭酸カルシウム粒子を含むウレタン樹脂溶液中には、前記の酸化アルミニウムなどの微粒子や顔料、架橋剤、触媒、酸化防止剤、紫外線吸収剤などの有機微粒子なども添加してもよい。
The urethane resin solution containing calcium carbonate particles to be applied to the fiber fabric includes the above urethane resin and calcium carbonate particles, and a water-soluble solvent such as dimethylformamide (hereinafter DMF), dimethylacetamide, N-methylpyrrolidone as a solvent. Those mainly composed of a polar organic solvent are preferably selected.
In the urethane resin solution containing the calcium carbonate particles, fine particles such as aluminum oxide, organic fine particles such as pigments, crosslinking agents, catalysts, antioxidants, and ultraviolet absorbers may be added.

この樹脂溶液を繊維布帛に対し、ナイフコ−タ、バ−コ−タ、コンマ−コ−タなどを用い繊維布帛に付与する。
次に、水のみまたは5〜20%程度のウレタン樹脂溶液で用いたDMFなどの有機溶媒を含んだ水中に、ウレタン樹脂溶液を塗布した繊維布帛を浸漬し、ウレタン樹脂を凝固させる。凝固温度は、樹脂膜中に形成される微多孔の孔径を適度に調整する観点から、10〜50℃の範囲が好ましい。
The resin solution is applied to the fiber fabric using a knife coater, bar coater, comma coater or the like.
Next, the fiber fabric coated with the urethane resin solution is immersed in water containing water or an organic solvent such as DMF used in a 5 to 20% urethane resin solution to solidify the urethane resin. The solidification temperature is preferably in the range of 10 to 50 ° C. from the viewpoint of appropriately adjusting the diameter of the microporous pores formed in the resin film.

次に、脱溶媒を行う。脱溶媒としては、水が好ましく、脱溶媒の温度は、10〜80℃の範囲が好ましく選択される。脱溶媒した後、90℃から150℃程度で乾燥を行う。
この後、必要に応じ、撥水加工や制電加工、撥水加工、抗菌防臭加工、制菌加工、紫外線遮蔽加工などをおこなってもよい。
また、微多孔質膜に加え、微多孔質膜上の全面に更にウレタン樹脂膜を付与する場合には、
Next, desolvation is performed. As the solvent removal, water is preferable, and the temperature of solvent removal is preferably selected in the range of 10 to 80 ° C. After removing the solvent, drying is performed at about 90 to 150 ° C.
Thereafter, if necessary, water-repellent processing, anti-static processing, water-repellent processing, antibacterial and deodorizing processing, antibacterial processing, ultraviolet shielding processing and the like may be performed.
Moreover, in addition to the microporous film, when further applying a urethane resin film to the entire surface of the microporous film,

(1)離型紙上に、ウレタン樹脂溶液を塗布、乾燥し、ウレタン樹脂膜を形成した後、離型紙上に得られたウレタン樹脂膜上に接着剤を塗布し、この接着剤を介し、微多孔膜と無孔質のウレタン樹脂膜を貼り合わせる。その後、必要に応じ30〜80℃で4時間〜100時間程度エ−ジングした後、離型紙を剥離するラミネ−ト法や
(2)微多孔質膜上に、ウレタン樹脂溶液をナイフコ−タやパイプコ−タなどで塗布、乾燥し、ウレタン樹脂膜を付与するダイレクトコ−ティング法
などにより、微多孔質膜上に、他のウレタン樹脂膜を付与することができる。
(1) A urethane resin solution is applied and dried on a release paper to form a urethane resin film, and then an adhesive is applied on the urethane resin film obtained on the release paper. A porous film and a nonporous urethane resin film are bonded together. Thereafter, after aging at 30 to 80 ° C. for about 4 to 100 hours as necessary, a laminating method in which the release paper is peeled off, or (2) a urethane resin solution is applied onto the microporous film by a knife coater or Other urethane resin films can be applied onto the microporous film by a direct coating method in which a urethane resin film is applied and dried by a pipe coater or the like.

また、微多孔質膜上の部分的にウレタン樹脂膜を付与する場合には、微多孔質膜上にグラビアコ−タやスクリ−ン捺染機を用い、点状や線状、菱形やその他の柄上にウレタン樹脂溶液を塗布し乾燥すればよい。
また、微多孔質膜上に他のウレタン樹脂膜を付与した後、必要に応じ、撥水加工や制電加工、撥水加工、抗菌防臭加工、制菌加工、紫外線遮蔽加工、カレンダ−加工などをおこなってもよい。
In addition, when a urethane resin film is partially applied on the microporous film, a gravure coater or a screen printing machine is used on the microporous film, and dot-like, linear, diamond-like or other A urethane resin solution may be applied on the handle and dried.
Also, after applying another urethane resin film on the microporous film, water repellent finish, anti-static finish, water repellent finish, antibacterial deodorizing finish, antibacterial finish, UV shielding finish, calendar finish etc. You may do.

以下、実施例により本発明を更に説明するが、本発明はこれらの実施例によりなんら限定されるものではない。また、例中の「部」は質量部である。
以下の実施例における評価は次の方法によった。
EXAMPLES Hereinafter, although an Example demonstrates this invention further, this invention is not limited at all by these Examples. Moreover, "part" in an example is a mass part.
Evaluation in the following examples was based on the following method.

A 層の厚み
電子顕微鏡による観察により測定をおこなった。
B 透湿度
酢酸カリウム法 JIS L1099−1993B−1法にて測定した。
塩化カルシウム法 JIS L1099−1993A−1法にて測定した。
なお、塩化カルシウム法、酢酸カルシウム法ともに、24時間当りの透湿量に換算した。
The thickness of the layer A was measured by observation with an electron microscope.
B Measured by moisture permeability potassium acetate method JIS L1099-1993B-1 method.
Calcium chloride method Measured by JIS L1099-1993A-1 method.
The calcium chloride method and the calcium acetate method were both converted to moisture permeation per 24 hours.

C 耐水圧
JIS L1092−1998耐水度試験(静水圧法)B法(高水圧法)に準じた方法で測定した。
水圧をかけることにより試験片が伸びる場合には、試験片の上にナイロンタフタ(2.54cm当りの縦糸と横糸の密度の合計が210本程度のもの)を重ねて、試験機に取り付けて測定をおこなった。
D 微多孔質膜中の粒子、微粒子の観察
電子顕微鏡により観察をおこなった。
E 風合
手でさわって判断を行なった。
C Water pressure resistance Measured by a method according to JIS L1092-1998 water resistance test (hydrostatic pressure method) B method (high water pressure method).
When the test piece is stretched by applying water pressure, nylon taffeta (with a total of about 210 warp and weft densities per 2.54 cm) is stacked on the test piece and attached to the tester. I did it.
D Observation of particles and fine particles in the microporous film Observation was performed with an electron microscope.
E Judged by touching hands.

実施例1
ポリエステルタフタ(たて糸83デシテッス/72フィラメント、よこ糸たて糸83デシテッス/72フィラメント。密度 たて114本/2.54cm、よこ92本/2.54cm)を分散染料で青色に染色し、フッ素系撥水剤アサヒガ−ドAG710 5%水溶液を用い撥水加工をおこなった後、170℃、圧力(線圧)128kg/cmにてカレンダ−加工したものを繊維布帛として用いた。
Example 1
Polyester taffeta (warp yarn 83 decites / 72 filaments, weft warp yarn 83 decites / 72 filaments, density 114 / 2.54 cm, weft 92 / 2.54 cm) dyed blue with disperse dye, fluorine-based water repellent A fiber fabric was used that was subjected to water repellent treatment using a 5% aqueous solution of Asahi Guard AG710 and calendered at 170 ° C. and a pressure (linear pressure) of 128 kg / cm.

次に下記樹脂溶液をパイプコ−タを用い0.15mmの厚みに繊維布帛に塗布し、15%のDMFを含む水中に浸漬し、ウレタン樹脂を凝固し、40℃の水中及び20℃の水中にて脱溶媒を行った後、120℃にて3分間乾燥、150℃にて1分間セットを行い。繊維布帛の片面に炭酸カルシウムを含む厚さ35μmの微多孔質膜を形成した。   Next, the following resin solution was applied to a fiber fabric to a thickness of 0.15 mm using a pipe coater, immersed in water containing 15% DMF, solidified with urethane resin, and immersed in 40 ° C. water and 20 ° C. water. After removing the solvent, it was dried at 120 ° C. for 3 minutes and set at 150 ° C. for 1 minute. A microporous film having a thickness of 35 μm and containing calcium carbonate was formed on one side of the fiber fabric.

樹脂溶液
エステル系ポリウレタン樹脂(固形分 25%) 100部
DMF 20部
炭酸カルシウム分散品 20部
(平均一次粒子径 0.7μm 分散後平均粒子径 1.0μm 固形分60%)
イソシアネ−ト系架橋剤 2部

得られた透湿性防水布帛の透湿度、耐水圧等を以下に記す。
Resin solution Ester-based polyurethane resin (solid content 25%) 100 parts DMF 20 parts Calcium carbonate dispersion 20 parts (average primary particle size 0.7 μm average particle size after dispersion 1.0 μm solid content 60%)
Isocyanate-based crosslinking agent 2 parts

The moisture permeability, water pressure resistance and the like of the obtained moisture permeable waterproof fabric are described below.

透湿度 塩化カルシウム法 10090g/m・24hrs
酢酸カリウム法 11300g/m・24hrs
耐水圧 160kPa
微多孔質膜中の粒子の観察 1μm前後の粒子が多数確認された。
風合 柔らかい。
Moisture permeability Calcium chloride method 10090g / m 2 · 24hrs
Potassium acetate method 11300 g / m 2 · 24 hrs
Water pressure resistance 160 kPa
Observation of particles in the microporous membrane Many particles around 1 μm were confirmed.
The texture is soft.

比較例1
実施例1の樹脂溶液から、炭酸カルシウム粒子を除いた以外は実施例1と同様にし、透湿性防水布帛を得た。
得られた透湿性防水布帛の透湿度、耐水圧等を以下に記す。
Comparative Example 1
A moisture-permeable waterproof fabric was obtained in the same manner as in Example 1 except that the calcium carbonate particles were removed from the resin solution of Example 1.
The moisture permeability, water pressure resistance and the like of the obtained moisture permeable waterproof fabric are described below.

透湿度 塩化カルシウム法 3500g/m・24hrs
酢酸カリウム法 2600g/m・24hrs
耐水圧 130kPa
微多孔質膜中の粒子の観察 粒子は確認されなかった。
風合 柔らかい。
Moisture permeability Calcium chloride method 3500g / m 2 · 24hrs
Potassium acetate method 2600g / m 2 · 24hrs
Water pressure resistance 130 kPa
Observation of particles in the microporous membrane No particles were observed.
The texture is soft.

実施例2
実施例1で用いた樹脂溶液に代えて下記を用いた以外は実施例1と同様にし、透湿性防水布帛を得た。
樹脂溶液
エステル系ポリウレタン樹脂(固形分 25%) 100部
DMF 20部
炭酸カルシウム分散品 20部
(平均一次粒子径 0.7μm 分散後平均粒子径 1.0μm 固形分60%)
酸化アルミニウム 7部
(平均一次粒子径 13nm 分散後平均粒子径 0.2μm 固形分14%)
イソシアネ−ト系架橋剤 2部
得られた透湿性防水布帛の透湿度、耐水圧等を以下に記す。
Example 2
A moisture-permeable waterproof fabric was obtained in the same manner as in Example 1 except that the following was used instead of the resin solution used in Example 1.
Resin solution Ester-based polyurethane resin (solid content 25%) 100 parts DMF 20 parts Calcium carbonate dispersion 20 parts (average primary particle size 0.7 μm average particle size after dispersion 1.0 μm solid content 60%)
7 parts of aluminum oxide (average primary particle size 13 nm, average particle size after dispersion 0.2 μm, solid content 14%)
The moisture permeability, water pressure resistance, etc. of the moisture permeable waterproof fabric obtained by 2 parts of the isocyanate-based crosslinking agent are described below.

透湿度 塩化カルシウム法 10210g/m・24hrs
酢酸カリウム法 21300g/m・24hrs
耐水圧 160kPa
微多孔質膜中の粒子の観察 1μm及び0.2μm前後の粒子が多数確認された。
風合 柔らかい。
Moisture permeability Calcium chloride method 10210 g / m 2 · 24 hrs
Potassium acetate method 21300g / m 2 · 24hrs
Water pressure resistance 160 kPa
Observation of particles in the microporous membrane Many particles having a size of about 1 μm and about 0.2 μm were confirmed.
The texture is soft.

実施例3
実施例1で用いた樹脂溶液に代えて下記を用いた以外は実施例1と同様にし、透湿性防水布帛を得た。
樹脂溶液
エステル系ポリウレタン樹脂(固形分 25%) 100部
DMF 20部
炭酸カルシウム分散品 20部
(平均一次粒子径 30nm 分散後平均粒子径3.0μm 固形分40%)
酸化アルミニウム 3部
(平均一次粒子径 13nmの凝集物 分散後平均粒子径0.5μm 固形分14%)
イソシアネ−ト系架橋剤 2部
得られた透湿性防水布帛の透湿度、耐水圧等を以下に記す。
Example 3
A moisture-permeable waterproof fabric was obtained in the same manner as in Example 1 except that the following was used instead of the resin solution used in Example 1.
Resin solution Ester polyurethane resin (solid content 25%) 100 parts DMF 20 parts Calcium carbonate dispersion 20 parts (average primary particle size 30 nm after dispersion average particle size 3.0 μm solid content 40%)
3 parts of aluminum oxide (aggregate having an average primary particle size of 13 nm, average particle size after dispersion of 0.5 μm, solid content of 14%)
The moisture permeability, water pressure resistance, etc. of the moisture permeable waterproof fabric obtained by 2 parts of the isocyanate-based crosslinking agent are described below.

透湿度 塩化カルシウム法 10090g/m・24hrs
酢酸カリウム法 17400g/m・24hrs
耐水圧 160kPa
微多孔質膜中の粒子の観察 0.1〜0.6μm前後の粒子が多数確認された。
風合 柔らかい。
Moisture permeability Calcium chloride method 10090g / m 2 · 24hrs
Potassium acetate method 17400 g / m 2 · 24 hrs
Water pressure resistance 160 kPa
Observation of particles in the microporous membrane A large number of particles of about 0.1 to 0.6 μm were confirmed.
The texture is soft.

実施例4
ポリエステルタフタ(たて糸83デシテッス/72フィラメント、よこ糸たて糸83デシテッス/72フィラメント。密度 たて114本/2.54cm、よこ92本/2.54cm)を分散染料で青色に染色し、フッ素系撥水剤アサヒガ−ドAG710 5%水溶液を用い撥水加工をおこなった後、170℃、圧力(線圧)128kg/cmにてカレンダ−加工したものを繊維布帛として用いた。
Example 4
Polyester taffeta (warp yarn 83 decites / 72 filaments, weft warp yarn 83 decites / 72 filaments, density 114 / 2.54 cm, weft 92 / 2.54 cm) dyed blue with disperse dye, fluorine-based water repellent A fiber fabric was used that was subjected to water repellent treatment using a 5% aqueous solution of Asahi Guard AG710 and calendered at 170 ° C. and a pressure (linear pressure) of 128 kg / cm.

次に下記樹脂溶液をパイプコ−タを用い0.15mmの厚みに繊維布帛に塗布し、15%のDMFを含む水中に浸漬し、ウレタン樹脂を凝固し、40℃の水中及び20℃の水中にて脱溶媒を行った後、120℃にて3分間乾燥、150℃にて1分間セットを行い。繊維布帛の片面に炭酸カルシウムを含む厚さ20μmの微多孔質膜を形成した。   Next, the following resin solution was applied to a fiber fabric to a thickness of 0.15 mm using a pipe coater, immersed in water containing 15% DMF, solidified with urethane resin, and immersed in 40 ° C. water and 20 ° C. water. After removing the solvent, it was dried at 120 ° C. for 3 minutes and set at 150 ° C. for 1 minute. A microporous film having a thickness of 20 μm and containing calcium carbonate was formed on one side of the fiber fabric.

樹脂溶液
エステル系ポリウレタン樹脂(固形分 25%) 100部
DMF 20部
炭酸カルシウム分散品 20部
(平均一次粒子径 0.7μm 分散後平均粒子径 1.0μm 固形分60%)
二酸化ケイ素分散品(表面がジメチルシリル基で疎水処理されたもの) 5部
(平均一次粒子径 0.02μm 分散後平均粒子径 1.0μm 固形分15%)
イソシアネ−ト系架橋剤 2部

得られた透湿性防水布帛の透湿度、耐水圧等を以下に記す。
Resin solution Ester-based polyurethane resin (solid content 25%) 100 parts DMF 20 parts Calcium carbonate dispersion 20 parts (average primary particle size 0.7 μm average particle size after dispersion 1.0 μm solid content 60%)
Silicon dioxide dispersion (surface treated with dimethylsilyl group for hydrophobic treatment) 5 parts (average primary particle size 0.02 μm, average particle size after dispersion 1.0 μm, solid content 15%)
Isocyanate-based crosslinking agent 2 parts

The moisture permeability, water pressure resistance and the like of the obtained moisture permeable waterproof fabric are described below.

透湿度 塩化カルシウム法 9800g/m・24hrs
酢酸カリウム法 16500g/m・24hrs
耐水圧 140kPa
微多孔質膜中の粒子の観察 1μm前後の粒子が多数確認された。
風合 柔らかい。
Moisture permeability Calcium chloride method 9800g / m 2 · 24hrs
Potassium acetate method 16500 g / m 2 · 24 hrs
Water pressure resistance 140kPa
Observation of particles in the microporous membrane Many particles around 1 μm were confirmed.
The texture is soft.

実施例5
ポリエステルタフタ(たて糸83デシテッス/72フィラメント、よこ糸たて糸83デシテッス/72フィラメント。密度 たて114本/2.54cm、よこ92本/2.54cm)を分散染料で青色に染色し、アサヒガ−ドAG710 5%水溶液を用い撥水加工をおこなった後、170℃、圧力(線圧)128kg/cmにてカレンダ−加工したものを繊維布帛として用いた。
Example 5
Polyester taffeta (warp warp 83 decites / 72 filaments, weft warp 83 decites / 72 filaments, density 114 / 2.54 cm, weft 92 / 2.54 cm) dyed blue with disperse dye, Asahi Guard AG710 5 A water-repellent treatment was performed using a 100% aqueous solution, and then calendered at 170 ° C. and a pressure (linear pressure) of 128 kg / cm was used as the fiber fabric.

次に下記樹脂溶液を塗布し、15%のDMFを含む水中に浸漬し、ウレタン樹脂を凝固し、40℃の水中及び20℃の水中にて脱溶媒を行った後、120℃にて3分間乾燥を行い。繊維布帛の片面に炭酸カルシウムを含む厚さ20μmの微多孔質膜を形成した。   Next, the following resin solution was applied, immersed in water containing 15% DMF, the urethane resin was coagulated, desolvated in 40 ° C. water and 20 ° C. water, and then at 120 ° C. for 3 minutes. Perform drying. A microporous film having a thickness of 20 μm and containing calcium carbonate was formed on one side of the fiber fabric.

樹脂溶液
エステル系ポリウレタン樹脂(固形分 25%) 100部
DMF 20部
炭酸カルシウム 20部
(平均一次粒子径 0.7μm 分散後平均粒子径 1.0μm 固形分60%)
イソシアネ−ト系架橋剤 2部
次に、離型紙上に下記樹脂溶液をバイプコ−タを用い塗布し、120℃にて乾燥して、厚さ15μmの無孔質のウレタン樹脂膜を得た。
Resin solution Ester-based polyurethane resin (solid content 25%) 100 parts DMF 20 parts Calcium carbonate 20 parts (average primary particle size 0.7 μm average particle size after dispersion 1.0 μm solid content 60%)
2 parts of isocyanate-based cross-linking agent Next, the following resin solution was applied onto a release paper using a vip coater and dried at 120 ° C. to obtain a non-porous urethane resin film having a thickness of 15 μm.

樹脂溶液(無孔質のウレタン樹脂膜用)
エ−テル系ポリウレタン樹脂(固形分30%) 100部
メチルエチルケトン 30部
白色顔料 8部
Resin solution (for non-porous urethane resin film)
Ether polyurethane resin (solid content 30%) 100 parts Methyl ethyl ketone 30 parts White pigment 8 parts

次に接着剤用の下記樹脂溶液をグラビアコ−タを用い無孔質のウレタン樹脂膜上に点状に付与した。
樹脂溶液(接着剤用)
エ−テル・エステル系ポリウレタン樹脂(固形分45%) 100部
トルエン 30部
イソシアネ−ト系架橋剤 9部
アミン系触媒 0.3部
Next, the following resin solution for the adhesive was applied in a spot shape on a nonporous urethane resin film using a gravure coater.
Resin solution (for adhesive)
Ether ester polyurethane resin (solid content 45%) 100 parts Toluene 30 parts Isocyanate crosslinking agent 9 parts Amine catalyst 0.3 part

次に、繊維布帛上に形成された微多孔質膜と無孔質膜を接着剤を介して貼り合わせ、60℃にて72時間エ−ジングをおこなった。
次に、離型紙を剥離した後、繊維布帛の表面にグラビアコ−タを用い、フッ素系撥水剤アサヒガ−ドAG710 5%水溶液を用い撥水加工をおこない透湿性防水布帛を得た。
得られた透湿性防水布帛の透湿度、耐水圧等を以下に記す。
Next, the microporous film and the nonporous film formed on the fiber fabric were bonded together with an adhesive and aged at 60 ° C. for 72 hours.
Next, after releasing the release paper, a gravure coater was used on the surface of the fiber cloth, and a water repellent treatment was performed using a 5% aqueous solution of a fluorine-based water repellent Asahigard AG710 to obtain a moisture permeable waterproof cloth.
The moisture permeability, water pressure resistance and the like of the obtained moisture permeable waterproof fabric are described below.

透湿度 塩化カルシウム法 5200g/m・24hrs
酢酸カリウム法 11300g/m・24hrs
耐水圧 320kPa
微多孔質膜中の粒子の観察 1μm前後の粒子が多数確認された。
風合 柔らかい。
Moisture permeability Calcium chloride method 5200g / m 2 · 24hrs
Potassium acetate method 11300 g / m 2 · 24 hrs
Water pressure resistance 320 kPa
Observation of particles in the microporous membrane Many particles around 1 μm were confirmed.
The texture is soft.

Claims (7)

繊維布帛の少なくとも片面に微多孔質膜を含むウレタン樹脂被膜が形成された透湿性防水布帛であって、前記微多孔質膜中に炭酸カルシウム粒子を含むことを特徴とする透湿性防水布帛。   A moisture-permeable waterproof fabric in which a urethane resin coating including a microporous membrane is formed on at least one surface of a fiber fabric, wherein the microporous membrane includes calcium carbonate particles. 前記微多孔質膜を形成するウレタン樹脂100質量に対し、前記炭酸カルシウム粒子が質量比で10質量部〜100質量部含むことを特徴とする請求項1記載の透湿性防水布帛。   2. The moisture-permeable waterproof fabric according to claim 1, wherein the calcium carbonate particles contain 10 to 100 parts by mass with respect to 100 parts by mass of the urethane resin forming the microporous membrane. 前記炭酸カルシウム粒子の平均粒子径が0.05μm〜5μmであることを特徴とする請求項1または2記載の透湿性防水布帛。 3. The moisture-permeable waterproof fabric according to claim 1, wherein the calcium carbonate particles have an average particle diameter of 0.05 μm to 5 μm. 前記微多孔質膜中に、酸化アルミニウム微粒子もしくは二酸化ケイ素微粒子をも含むことを特徴とする請求項1〜3いずれかに記載の透湿性防水布帛。   The moisture-permeable waterproof fabric according to any one of claims 1 to 3, wherein the microporous film also contains aluminum oxide fine particles or silicon dioxide fine particles. 前記炭酸カルシウム100質量部に対し、前記アルミニウム微粒子もしくは前記二酸化ケイ素微粒子が質量比で0.1〜30質量部含むことを特徴とする請求項4記載の透湿性防水布帛。   The moisture-permeable waterproof fabric according to claim 4, wherein the aluminum fine particles or the silicon dioxide fine particles are contained in an amount of 0.1 to 30 parts by mass with respect to 100 parts by mass of the calcium carbonate. 耐水圧が100kPa以上200kPa以下であり、塩化カルシウム法による透湿度が8000g/m・24hrs以上15000g/m・24hrs以下、酢酸カリウム法による透湿度が10000g/m・24hrs以上30000g/m・24hrs以下であることを特徴とする請求項1〜5いずれかに記載の透湿性防水布帛。 Water pressure is below 200kPa than 100 kPa, moisture permeability 8000g / m 2 · 24hrs or more 15000g / m 2 · 24hrs or less by the calcium chloride method, the moisture permeability with potassium acetate method is 10000g / m 2 · 24hrs or more 30 000 g / m 2 -The moisture-permeable waterproof fabric according to any one of claims 1 to 5, which is 24 hrs or less. 繊維布帛に、炭酸カルシウム粒子を含むウレタン樹脂溶液を塗布した後、水中に浸漬し、ウレタン樹脂を凝固させることを特徴とする透湿性防水布帛の製造方法。   A method for producing a moisture-permeable waterproof fabric, characterized in that a urethane resin solution containing calcium carbonate particles is applied to a fiber fabric and then immersed in water to solidify the urethane resin.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9206546B2 (en) 2009-05-01 2015-12-08 Seiren Co., Ltd. Moisture-permeable waterproof fabric and process for producing same

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JPH06136320A (en) * 1992-10-26 1994-05-17 Mitsubishi Kasei Corp Production of moisture-permeable waterproof coated molding
JPH06272168A (en) * 1993-03-22 1994-09-27 Unitika Ltd Moisture-permeable and waterproof-coated fabric
JPH06313275A (en) * 1993-04-28 1994-11-08 Komatsu Seiren Kk Moisture-permeable waterproof fabric and its production
JPH09158051A (en) * 1995-12-13 1997-06-17 Seiren Co Ltd Moisture permeable and water proofing coated fabric and its production
JPH1161648A (en) * 1997-08-14 1999-03-05 Komatsu Seiren Kk Moisture-permeable and waterproof fabric

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06136320A (en) * 1992-10-26 1994-05-17 Mitsubishi Kasei Corp Production of moisture-permeable waterproof coated molding
JPH06272168A (en) * 1993-03-22 1994-09-27 Unitika Ltd Moisture-permeable and waterproof-coated fabric
JPH06313275A (en) * 1993-04-28 1994-11-08 Komatsu Seiren Kk Moisture-permeable waterproof fabric and its production
JPH09158051A (en) * 1995-12-13 1997-06-17 Seiren Co Ltd Moisture permeable and water proofing coated fabric and its production
JPH1161648A (en) * 1997-08-14 1999-03-05 Komatsu Seiren Kk Moisture-permeable and waterproof fabric

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9206546B2 (en) 2009-05-01 2015-12-08 Seiren Co., Ltd. Moisture-permeable waterproof fabric and process for producing same

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